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Imidazo[1,2-a]pyridine

SYNTHESIS OF NOVEL IMIDAZO [1, 2 a] PYRIDINE FOR THEIR POTENT ANTI CONVULSANT ACTIVITY

SYNTHESIS OF NOVEL IMIDAZO [1, 2 a] PYRIDINE FOR THEIR POTENT ANTI CONVULSANT ACTIVITY

... beings. Imidazo[1,2-a]pyridine are having the number of biological ...etc. Imidazo[1,2-a] pyridine showed diversified pharmacological ...of Imidazo[1,2-a]pyridine, it was ...

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Structural characterization and Hirshfeld surface analysis of a CoII complex with imidazo[1,2 a]pyridine

Structural characterization and Hirshfeld surface analysis of a CoII complex with imidazo[1,2 a]pyridine

... water (20 ml) yielding a clear pink solution. A hot water– methanol (1:1) solution (20 ml) of imidazo[1,2-a]pyridine (1.0 mmol, 0.118 g) was added dropwise to the above solution under ...

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SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL SCREENING OF NOVEL SERIES OF IMIDAZO[1,2 a]PYRIDINE DERIVATIVES LINKED TO SECONDARY AMINES

SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL SCREENING OF NOVEL SERIES OF IMIDAZO[1,2 a]PYRIDINE DERIVATIVES LINKED TO SECONDARY AMINES

... of 2-(4-Fluorophenyl)-6-methyl-3-(N,N- dialkylamine-4-ylmethyl)imidazo[1,2-a]pyridines (IP-1 TO IP-10): To a solution of 2-(4- fluorophenyl)-6-methylH-imidazo[1,2-a]pyridine ...

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MICROWAVE ASSISTED SYNTHESIS OF IMIDAZO[1,2 a]PYRIDINE DERIVATIVES AND THEIR ANTI INFLAMMATORY ACTIVITY

MICROWAVE ASSISTED SYNTHESIS OF IMIDAZO[1,2 a]PYRIDINE DERIVATIVES AND THEIR ANTI INFLAMMATORY ACTIVITY

... the imidazo[1,2-a]pyridine derivatives were screened for their anti- inflammatory property ...synthesized imidazo[1,2-a] pyridine derivatives showed anti-inflammatory potential which might be ...

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Crystal structure, DFT calculation, Hirshfeld surface analysis and energy framework study of 6 bromo 2 (4 bromo­phen­yl)imidazo[1,2 a]pyridine

Crystal structure, DFT calculation, Hirshfeld surface analysis and energy framework study of 6 bromo 2 (4 bromo­phen­yl)imidazo[1,2 a]pyridine

... single-step reaction method. The title molecule is planar, showing a dihedral angle of 0.62 (17) between the phenyl and the imidazo[1,2-a] pyridine rings. An intramolecular C—H N hydrogen bond with an S(5) ...

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Synthesis and antibacterial activity of novel imidazo[1,2 a]pyrimidine and imidazo[1,2 a]pyridine chalcones derivatives

Synthesis and antibacterial activity of novel imidazo[1,2 a]pyrimidine and imidazo[1,2 a]pyridine chalcones derivatives

... Similarly, imidazo pyrimidine nucleus possesses important therapeutics such as calcium antagonists, anticancer agents, antifungal activity anti-inflammatory and analgesic ...available 2-aminopyrimidine and ...

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Synthesis and antimicrobial activity of some new Imidazo[1,2 a]pyridine derivatives

Synthesis and antimicrobial activity of some new Imidazo[1,2 a]pyridine derivatives

... properties. Imidazo[1,2-a]pyridine also act as selective cyclin-dependant kinase inhibitors[4], GABA and benzodiazepine receptor agonists[5], and cardiotonic ...containing ...

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Synthesis and Antimicrobial screening of Chalcones containing imidazo [1,2-a] pyridine nucleus

Synthesis and Antimicrobial screening of Chalcones containing imidazo [1,2-a] pyridine nucleus

... Recently, imidazo [1,2-a] pyridines have significant importance in the pharmaceutical industry 1 owing to their various interesting biological activity displayed over a broad range of therapeutic classes; ...

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Fluorescent property of 3-hydroxymethyl imidazo[1,2-a]pyridine and pyrimidine derivatives

Fluorescent property of 3-hydroxymethyl imidazo[1,2-a]pyridine and pyrimidine derivatives

... of imidazo[1,2-a]pyrimidines and pyridines has been devel- oped due to the extent of their applications in pharmaco- logical ...ever, imidazo[1,2-a]pyridines and pyrimidines are also at- tractive due to ...

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DESIGN AND SYNTHESIS OF NOVEL IMIDAZO[1,2 A]PYRIDINE DERIVATIVES AND THEIR ANTI BACTERIAL ACTIVITY

DESIGN AND SYNTHESIS OF NOVEL IMIDAZO[1,2 A]PYRIDINE DERIVATIVES AND THEIR ANTI BACTERIAL ACTIVITY

... infrared, mass spectral analysis, and screened for their antibacterial activity by disc diffusion method. Molecular docking studies were performed with a bacterial beta subunit of DNA gyrase using Auto Dock 4.2.6, and ...

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Identification of novel Imidazo[1,2 a]pyridine inhibitors targeting M  tuberculosis QcrB

Identification of novel Imidazo[1,2 a]pyridine inhibitors targeting M tuberculosis QcrB

... the imidazo[1,2-a]pyridine-3-nitroso compounds, but they exhibit undesirable toxicity in a VERO cell line ...the imidazo[1,2-a]pyridine-3-hydrazones, have been synthesized but are all inactive ...

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6 Bromo 3 (2 methyl­propen­yl)imidazo[1,2 a]pyridine

6 Bromo 3 (2 methyl­propen­yl)imidazo[1,2 a]pyridine

... Imidazo[1,2-a]pyridine derivatives are important inter- mediates in organic synthesis, especially in the synthesis of biologically active and medicinally useful agents. For instance, they are widely used in ...

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2 (3 Bromo 4 meth­oxy­phen­yl)imidazo[1,2 a]pyridine

2 (3 Bromo 4 meth­oxy­phen­yl)imidazo[1,2 a]pyridine

... Imidazo[1,2-a]pyridine and its derivatives have clinical appli- cations in the treatment of anxiety disorders; Alpidem (Georges et al., 1993) and Zolpidem (Depoortere et al.,1986) are in this category. The ...

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2 Methyl 6 (tri­fluoro­meth­yl)imidazo[1,2 a]pyridine 3 carbo­nitrile

2 Methyl 6 (tri­fluoro­meth­yl)imidazo[1,2 a]pyridine 3 carbo­nitrile

... that imidazo[1,2-a]pyridine derivatives exhibit diverse biological activities (Gudmundsson & Johns, 2003) and were used as antiviral (Elhakmoui et ...

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Aqueous phase synthesis of substituted imidazo[1,2 a]pyridine in the presence of β cyclodextrin

Aqueous phase synthesis of substituted imidazo[1,2 a]pyridine in the presence of β cyclodextrin

... with 2-aminopyridines (entry1,Table1),furnished the azaindolizines ...of 2-arylimidazo[1,2-a] pyridines as these methods12,18 needed refluxing in organic solvents for 6 ...of ...

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Catalyst Free Synthesis of 2-(3, 4-dichlorophenyl)-1, 8a-dihydroimidazo [1, 2-a] pyridine Derivatives as Potent Antimicrobial Agents

Catalyst Free Synthesis of 2-(3, 4-dichlorophenyl)-1, 8a-dihydroimidazo [1, 2-a] pyridine Derivatives as Potent Antimicrobial Agents

... Patients undergoing organ transplants, anticancer chemotherapy or long treatment with antimicrobial agents, as well as patients with AIDS are immuno suppressed and very susceptible to life threatening systemic microbial ...

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Reaction of Nitrilimines with 2 Aminopicoline, 3 Amino 1,2,4 Triazole, 5 Aminotetrazole and 2 Aminopyrimidine

Reaction of Nitrilimines with 2 Aminopicoline, 3 Amino 1,2,4 Triazole, 5 Aminotetrazole and 2 Aminopyrimidine

... produced imidazo[1,2-a]pyri- dines 7-10, while the reaction of the same picoline derivatives with hydrazonoylhalide 1b afforded imidazo[1,2-a]pyridine-2-ones ...MS, 1 HNMR and 13 ...

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Microwave assisted synthesis of bis and tris(ω-bromoacetophenones): versatile precursors for novel bis(imidazo[1,2-a]pyridines), bis(imidazo[1,2-a]pyrimidines) and their tris-analogs

Microwave assisted synthesis of bis and tris(ω-bromoacetophenones): versatile precursors for novel bis(imidazo[1,2-a]pyridines), bis(imidazo[1,2-a]pyrimidines) and their tris-analogs

... uses 2-aminopyridine or 2-aminopyrimidine, and α- halocarbonyl compound as starting ...are 2–4 times their respective boiling points and thus providing large rate enhance- ment ...

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Synthesis and antimicrobial studies of 2 (5 substituted) 1, 3, 4 oxadiazole 2 yl) H imidazo [1, 2, α] pyridine derivatives

Synthesis and antimicrobial studies of 2 (5 substituted) 1, 3, 4 oxadiazole 2 yl) H imidazo [1, 2, α] pyridine derivatives

... that imidazo [1, 2-a] pyridine derivatives exhibited diverse biological activities [1-3] and are used as antiviral, [4-12] antiulcer, [ 13-15] antibacterial, [16-17] antifungal, [18-19] ...

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Synthesis and Evaluation of Antituberculosis Activity of Substituted 2,7 Dimethylimidazo [1,2 a]Pyridine 3 Carboxamide Derivatives

Synthesis and Evaluation of Antituberculosis Activity of Substituted 2,7 Dimethylimidazo [1,2 a]Pyridine 3 Carboxamide Derivatives

... Various imidazo fused hetero- cycles with aryloxy alkylamines side chain including imidazo[1,2-a]pyridines act as cal- cium channel blockers or as local anaesthetics ...substituted ...

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